Canonical Allele Identifier: PA2827999030
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133523
ClinVar RCV Id: RCV000120033 RCV000230402 RCV000677760 RCV000774673 RCV000586315 RCV003315716 RCV003997330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr2552Ile
CA014100
NM_001354901.2:c.7655C>T